Note: Descriptions are shown in the official language in which they were submitted.
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1
MICROBICIDAL COMPOSITION
This invention relates to a synergistic combination of selected microbicides
having greater activity than would be observed for the individual
microbicides.
In some cases, commercial microbicides cannot provide effective control of
microorganisms, even at high use concentrations, due to weak activity against
certain types of microorganisms, e.g., those resistant to some microbicides,
or
due to aggressive environmental conditions. Combinations of different
microbicides are sometimes used to provide overall control of microorganisms
in
a particular end use environment. For example, U.S. Pat. App. Pub. No.
2007/0078118 discloses synergistic combinations of N-methyl-1,2-
benzisothiazolin-3-one (MBIT) with other biocides. However, there is a need
for
additional combinations of microbicides having enhanced activity against
various
strains of microorganisms to provide effective control of the microorganisms.
Moreover, there is a need for combinations containing lower levels of
individual
microbicides for environmental and economic benefit. The problem addressed by
this invention is to provide such additional combinations of microbicides.
STATEMENT OF THE INVENTION
The present invention is directed to a microbicidal composition
comprising: (a) N-methyl-1,2-benzisothiazolin-3-one; and (b) at least one
microbicide selected from the group consisting of ethyl lauroyl arginate
hydrochloride, cocamidopropyl-N-2-hydroxyethylcarbamoyl methyl dimethyl
ammonium chloride, Cu(II) 2-aminoethanolate and didecyl dimethyl ammonium
chloride, didecyl dimethyl ammonium carbonate and bicarbonate, Cu(II) 2-
aminoethanolate, glycerol monolaurate, propylene glycol mono-laurate, and
propylene glycol caprylate.
DETAILED DESCRIPTION OF THE INVENTION
As used herein, the following terms have the designated definitions,
unless the context clearly indicates otherwise. "MBIT" is N-methyl-1,2-
benzisothiazolin-3-one. The term "microbicide" refers to a compound capable of
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2
killing, inhibiting the growth of or controlling the growth of microorganisms
at a
locus; microbicides include bactericides, fungicides and algaecides. The term
"microorganism" includes, for example, fungi (such as yeast and mold),
bacteria
and algae. The term "locus" refers to an industrial system or product subject
to
contamination by microorganisms. The following abbreviations are used
throughout the specification: ppm = parts per million by weight
(weight/weight),
mL = milliliter, ATCC = American Type Culture Collection, MBC = minimum
biocidal concentration, and MIC = minimum inhibitory concentration. Unless
otherwise specified, temperatures are in degrees centigrade ( C), and
references
to percentages (%) are by weight. Amounts of organic microbicides are given on
an active ingredient basis in ppm (w/w).
The compositions of the present invention unexpectedly have been found
to provide enhanced microbicidal efficacy at a combined active ingredient
level
lower than that of the individual microbicides. Additional microbicides beyond
those listed in the claims may be present in the composition.
In one embodiment of the invention, the antimicrobial composition
comprises N-methyl-1,2-benzisothiazolin-3=one and ethyl lauroyl arginate
hydrochloride. Preferably, a weight ratio of ethyl lauroyl arginate
hydrochloride
to N-methyl-1,2-benzisothiazolin-3-one is from 1:94 to 1:0.0137.
In one embodiment of the invention, the antimicrobial composition
comprises N-methyl-1,2-benzisothiazolin-3-one and cocamidopropyl-N-2-
hydroxyethylcarbamoyl methyl dimethyl ammonium chloride. Preferably, a
weight ratio of cocamidopropyl-N-2-hydroxyethylcarbamoyl methyl dimethyl
ammonium chloride to N-methyl-1,2-benzisothiazolin-3-one is from 1:188 to
1:0.0022.
In one embodiment of the invention, the antimicrobial composition
comprises N-methyl-1,2-benzisothiazolin-3-one and Cu(II) 2-aminoethanolate
and didecyl dimethyl ammonium chloride. Preferably, a weight ratio of Cu(II) 2-
aminoethanolate and didecyl dimethyl ammonium chloride to N-methyl-1,2-
benzisothiazolin-3-one is from 1:176 to 1:0.08.
In one embodiment of the invention, the antimicrobial composition
comprises N-methyl-1,2-benzisothiazolin-3-one and didecyl dimethyl ammonium
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3
carbonate and bicarbonate. Preferably, a weight ratio of didecyl dimethyl
ammonium carbonate and bicarbonate to N-methyl-1,2-benzisothiazolin-3-one is
from 1:227 to 1:0.179.
In one embodiment of the invention, the antimicrobial composition
comprises N-methyl-1,2-benzisothiazolin-3-one and Cu(II) 2-aminoethanolate.
Preferably, a weight ratio of Cu(II) 2-aminoethanolate to N-methyl-1,2-
benzisothiazolin-3-one is from 1:375 to 1:0.004.
In one embodiment of the invention, the antimicrobial composition
comprises N-methyl-1,2-benzisothiazolin-3-one and glycerol monolaurate.
Preferably, a weight ratio of glycerol monolaurate to N-methyl-1,2-
benzisothiazolin-3-one is from 1:0.143 to 1:0.0004.
In one embodiment of the invention, the antimicrobial composition
comprises N-methyl-1,2-benzisothiazolin-3-one and propylene glycol mono-
laurate. Preferably, a weight ratio of propylene glycol mono-laurate to N-
methyl-
1,2-benzisothiazolin-3-one is from 1:0.286 to 1:0.0286.
In one embodiment of the invention, the antimicrobial composition
comprises N-methyl-1,2-benzisothiazolin-3-one and propylene glycol caprylate.
Preferably, a weight ratio of propylene glycol caprylate to N-methyl-1,2-
benzisothiazolin-3-one is from 1:0.442 to 1:0.0018.
The microbicides in the composition of this invention may be used "as is"
or may first be formulated with a solvent or a solid carrier. Suitable
solvents
include, for example, water; glycols, such as ethylene glycol, propylene
glycol,
diethylene glycol, dipropylene glycol, polyethylene glycol, and polypropylene
glycol; glycol ethers; alcohols, such as methanol, ethanol, propanol,
phenethyl
alcohol and phenoxypropanol; ketones, such as acetone and methyl ethyl ketone;
esters, such as ethyl acetate, butyl acetate, triacetyl citrate, and glycerol
triacetate; carbonates, such as propylene carbonate and dimethyl carbonate;
and
mixtures thereof. It is preferred that the solvent is selected from water,
glycols,
glycol ethers, esters and mixtures thereof. Suitable solid carriers include,
for
example, cyclodextrin, silicas, diatomaceous earth, waxes, cellulosic
materials,
alkali and alkaline earth (e.g., sodium, magnesium, potassium) metal salts
(e.g.,
chloride, nitrate, bromide, sulfate) and charcoal.
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When a microbicide component is formulated in a solvent, the formulation
may optionally contain surfactants. When such formulations contain
surfactants, they are generally in the form of emulsive concentrates,
emulsions,
microemulsive concentrates, or microemulsions. Emulsive concentrates form
emulsions upon the addition of a sufficient amount of water. Microemulsive
concentrates form microemulsions upon the addition of a sufficient amount of
water. Such emulsive and microemulsive concentrates are generally well known
in the art; it is preferred that such formulations are free of surfactants.
U.S.
Patent No. 5,444,078 may be consulted for further general and specific details
on
the preparation of various microemulsions and microemulsive concentrates.
A microbicide component also can be formulated in the form of a
dispersion. The solvent component of the dispersion can be an organic solvent
or
water, preferably water. Such dispersions can contain adjuvants, for example,
co-solvents, thickeners, anti-freeze agents, dispersants, fillers, pigments,
surfactants, biodispersants, sulfosuccinates, terpenes, furanones,
polycations,
stabilizers, scale inhibitors and anti-corrosion additives.
When both microbicides are each first formulated with a solvent, the
solvent used for the first microbicide may be the same as or different from
the
solvent used to formulate the other commercial microbicide, although water is
preferred for most industrial biocide applications. It is preferred that the
two
solvents are miscible.
Those skilled in the art will recognize that the microbicide components of
the present invention may be added to a locus sequentially, simultaneously, or
may be combined before being added to the locus. It is preferred that the
first
microbicide and the second microbicide component be added to a locus
simultaneously or sequentially. When the microbicides are added
simultaneously or sequentially, each individual component may contain
adjuvants, such as, for example, solvent, thickeners, anti-freeze agents,
colorants, sequestrants (such as ethylenediamine-tetraacetic acid,
ethylenediaminedisuccinic acid, iminodisuccinic acid and salts thereoD,
dispersants, surfactants, biodispersants, sulfosuccinates, terpenes,
furanones,
polycations, stabilizers, scale inhibitors and anti-corrosion additives.
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The microbicidal compositions of the present invention can be used to
inhibit the growth of microorganisms or higher forms of aquatic life (such as
protozoans, invertebrates, bryozoans, dinoflagellates, crustaceans, mollusks,
etc.)
by introducing a microbicidally effective amount of the compositions onto,
into, or
5 at a locus subject to microbial attack. Suitable loci include, for example:
industrial process water; electrocoat deposition systems,; cooling towers; air
washers; gas scrubbers,' mineral slurries; wastewater treatment; ornamental
fountains; reverse osmosis filtration; ultrafiltration; ballast water;
evaporative
condensers; heat exchangers; pulp and paper processing fluids and additives;
starch; plastics; emulsions; dispersions; paints; latices; coatings, such as
varnishes; construction products, such as mastics, caulks, and sealants;
construction adhesives, such as ceramic adhesives, carpet backing adhesives,
and
laminating adhesives; industrial or consumer adhesives; photographic
chemicals;
printing fluids; household products, such as bathroom and kitchen cleaners and
sanitary wipes; cosmetics; toiletries; shampoos; soaps; detergents; industrial
cleaners; floor polishes; laundry rinse water; metalworking fluids; conveyor
lubricants; hydraulic fluids; leather and leather products; textiles; textile
products; wood and wood products, such as plywood, chipboard, wallboard,
flakeboard, laminated beams, oriented strandboard, hardboard, and
particleboard; petroleum processing fluids; fuel; oilfield fluids, such as
injection
water, fracture fluids, and drilling muds; agriculture adjuvant preservation;
surfactant preservation; medical devices; diagnostic reagent preservation;
food
preservation, such as plastic or paper food wrap; food, beverage, and
industrial
process pasteurizers; toilet bowls; recreational water; pools; and spas.
Preferably, the microbicidal compositions of the present invention are used
to inhibit the growth of microorganisms at a locus selected from one or more
of
mineral slurries, pulp and paper processing fluids and additives, starch,
emulsions, dispersions, paints, latices, coatings, construction adhesives,
such as
ceramic adhesives, carpet backing adhesives, photographic chemicals, printing
fluids, household products such as bathroom and kitchen cleaners and sanitary
wipes, cosmetics, toiletries, shampoos, soaps, detergents, industrial
cleaners,
floor polishes, laundry rinse water, metal working fluids, textile products,
wood
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and wood products, agriculture adjuvant preservation, surfactant preservation,
diagnostic reagent preservation, food preservation, and food, beverage, and
industrial process pasteurizers.
The specific amount of the composition of this invention necessary to
inhibit or control the growth of microorganisms and higher aquatic life forms
in a
locus depends upon the particular locus to be protected. Typically, the amount
of
the composition of the present invention to control the growth of
microorganisms
in a locus is sufficient if it provides from 0.1 to 1,000 ppm of the
isothiazoline
ingredient of the composition in the locus. It is preferred that the
isothiazolone
ingredients of the composition be present in the locus in an amount of at
least 0.5
ppm, more preferably at least 4 ppm and most preferably at least 10 ppm. It'is
preferred that the isothiazolone ingredients of the composition be present in
the
locus in an amount of no more than 1000 ppm, more preferably no more than 500
ppm, and most preferably no more than 200 ppm.
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EXAMPLES
Materials and Methods
The synergism of the combination of the present invention was
demonstrated by testing a wide range of concentrations and ratios of the
compounds.
One measure of synergism is the industrially accepted method described
by Kull, F.C.; Eisman, P.C.; Sylwestrowicz, H.D. and Mayer, R.L., in Applied
Microbiology 9:538-541 (1961), using the ratio determined by the formula:
Qa/QA + Qb/QB = Synergy Index ("SI")
wherein:
QA = concentration of compound A (first component) in ppm, acting alone,
which produced an end point (MIC of Compound A).
Qa = concentration of compound A in ppm, in the mixture, which produced
an end point.
QB = concentration of compound B (second component) in ppm, acting
alone, which produced an end point (MIC of Compound B).
Qb = concentration of compound B in ppm, in the mixture, which produced
an end point.
When the sum of Qa/QA and Qb/QB is greater than one, antagonism is
indicated. When the sum is equal to one, additivity is indicated, and when
less
than one, synergism is demonstrated. The lower the SI, the greater the synergy
shown by that particular mixture. The minimum inhibitory concentration (MIC)
of a microbicide is the lowest concentration tested under a specific set of
conditions that prevents the growth of added microorganisms.
Synergy tests were conducted using standard microtiter plate assays with
media designed for optimal growth of the test microorganism. Minimal salt
medium supplemented with 0.2% glucose and 0.1% yeast extract (M9GY
medium) was used for testing bacteria; Potato Dextrose Broth (PDB medium)
was used for testing yeast and mold. In this method, a wide range of
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combinations of microbicides was tested by conducting high resolution MIC
assays in the presence of various concentrations of MBIT. High resolution MICs
were determined by adding varying amounts of microbicide to one column of a
microtitre plate and doing subsequent ten-fold dilutions using an automated
liquid handling system to obtain a series of endpoints ranging from 2 ppm to
10,000 ppm active ingredient.
The synergy of the combinations of the present invention was determined
against several microorganisms, as described in the Tables below. The bacteria
were used at a concentration of about 5 x 106 bacteria per mL and the yeast
and
mold at 5 x 105 fungi per mL. These microorganisms are representative of
natural contaminants in many consumer and industrial applications. The
plates were visually evaluated for microbial growth (turbidity) to determine
the
MIC after various incubation times at 25 C (yeast and mold) or 30 C
(bacteria).
The test results for demonstration of synergy of the MBIT combinations of
the present invention are shown below in Tables 1 through 8. In each test,
Second Component (B) was MBIT and the First Component (A) was the other
commercial microbicide. Each table shows the specific combinations of MBIT
and the other component; results against the microorganisms tested with
incubation times; the end-point activity in ppm measured by the MIC for MBIT
alone (QB), for the other component alone (QA), for MBIT in the mixture (Qb)
and
for the other component in the mixture (Qa); the calculated SI value; and the
range of synergistic ratios for each combination tested (other component/MBIT
or
A/B).
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Tablel
Ca: ppm Al of CYTO GUARD IA (ethyl lauroyl arginate hydrochloride)
Cb: ppm AI of MBIT(N-methyl-1,2-benzisothiazolin-3-one)
Ratio:Ca:Cb
Test Organisms Contact Ca Cb S.I. Ca:Cb
Time
A. niger 3 days 110 - - -
ATCC # 16404 - 37.5 - -
0.2 18.8 0.50 1:94.0000
2 18.8 0.52 1:9.4000
11 18.8 0.60 1:1.7091
20 18.8 0.68 1:0.9400
30 18.8 0.77 1:0.6267
42.5 18.8 0.89 1:0.4424
52.5 18.8 0.98 1:0.3581
65 18.8 1.09 1:0.2892
11 9.4 0.35 1:0.8545
20 9.4 0.43 1:0.4700
30 9.4 0.52 1Ø3133
42.5 9.4 0.64 1:0.2212
52.5 9.4 0.73 1:0.1790
65 9.4 0.84 1:0.1446
87.5 9.4 1.05 1:0.1074
42.5 4.7 0.51 1:0.1106
52.5 4.7 0.60 1:0.0895
65 4.7 0.72 1:0.0723
87.5 4.7 0.92 1:0.0537
110 4.7 1.13 1:0.0427
42.5 2.4 0.45 1:0.0565
52.5 2.4 0.54 1:0.0457
65 2.4 0.65 1:0.0369
87.5 2.4 0.86 1:0.0274
110 2.4 1.06 1:0.0218
42.5 1.2 0.42 1:0.0282
65 1.2 0.62 1:0.0185
87.5 1.2 0.83 1:0.0137
110 1.2 1.03 1:0.0109
7 days 110 - - -
- 37.5 - -
2 18.8 0.52 1:9.4000
11 18.8 0.6 1:1.7091
20 18.8 0.68 1:0.9400
30 18.8 0.77 1:0.6267
42.5 18.8 0.89 1:0.4424
52.5 18.8 0.98 1:0.3581
65 18.8 1.09 1:0.2892
20 9.4 0.43 1:0.4700
30 9.4 0.52 1:0.3133
42.5 9.4 0.64 1:0.2212
52.5 9.4 0.73 1:0.1790
65 9.4 0.84 1:0.1446
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87.5 9.4 1.05 1:0.1074
42.5 4.7 0.51 1:0.1106
52.5 4.7 0.6 1:0.0895
65 4.7 0.72 1:0.0723
87-5 4.7 ..92 1:0.0537
110 4.7 1.13 1:0.0427
42.5 2.4 0.45 1:0.0565
52.5 2.4 0.54 1:0.0457
65 2.4 0.65 1:0.0369
87.5 2.4 0.86 1:0.0274
110 2.4 1.06 1:0.0218
65 1.2 0.62 1:0.0185
87.5 1.2 0.83 1:0.0137
110 1.2 1.03 1:0.0109
C.albicans 48 hrs 87.5 - - -
ATCC # 10231 - 30 - -
6.5 15 0.57 1:2.3077
11 15 0.63 1:1.3636
15 0.73 1:0.7500
15 0.84 1:0.5000
42.5 15 0.99 1:0.3529
6.5 7.5 0.32 1:1.1538
11 7.5 0.38 1:0.6818
20 7.5 0.48 1:0.3750
30 7.5 0.59 1:0.2500
42.5 7.5 0.74 1:0.1765
52.5 7.5 0.85 1:0.1429
65 7.5 0.99 1:0.1154
8.75 3.75 0.23 1:0.4286
11 3.75 0.25 1:0.3409
20 3.75 0.35 1:0.1875
30 3.75 0.47 1:0.1250
42.5 3.75 0.61 1:0.0882
52.5 3.75 0.73 1:0.0714
65 3.75 0.87 1:0.0577
87.5 3.75 1.13 1:0.0429
20 1.86 0.29 1:0.0930
30 1.86 0.40 1:0.0620
42.5 1.86 0.55 1:0.0438
52.5 1.86 0.66 1:0.0354
65 1.86 0.80 1:0.0286
87.5 1.86 1.06 1:0.0213
87.5 0.94 1.03 1:0.0107
72 hrs 87.5 - - -
- 30 -
8.75 15 0.60 1:1.7143
11 15 0.63 1:1.3636
20 15 0.73 1:0.7500
30 15 0.84 1:0.5000
42.5 15 0.99 1=0.3529
8.75 7.5 0.35 1:0.8571
11 7.5 0.38 1:0.6818
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20 7.5 0.48 1:0.3750
30 7.5 0.59 1:0.2500
42.5 7.5 0.74 1:0.1765
52.5 7.5 0.85 1:0.1429
65 7.5 0.99 1:0.1154
11 3.75 0.25 1:0.3409
20 3.75 0.35 1:0.1875
30 3.75 0.47 1:0.1250
42.5 3.75 0.61 1:0.0882
52.5 3.75 0.73 1:0.0714
65 3.75 0.87 1:0.0577
87.5 3.75 1.13 1:0.0429
42.5 1.86 0.55 1:0.0438
52.5 1.86 0.66 1:0.0354
65 1.86 0.8 1:0.0286
87.5 1.86 1.06 1:0.0213
Ps. aeruginosa 48hrs 42.5
ATCC#9027 - 125 - -
30 18.75 0.86 1:0.6250
42.5 18.75 1.15 1:0.4412
30 9.4 0.78 1:0.3133
42.5 9.4 1.08 1:0.2212
30 4.6 0.74 1:0.1533
42.5 4.6 1.04 1:0.1082
42.5 2.3 1.02 1:0.0541
S.aureus 24hrs 2.125 - - -
ATCC#6538 - 15 - -
1 7.5 0.97 1:7.5000
1.5 7.5 1.21 1:5.0000
1 3.8 0.72 1:3.8000
1.5 3.8 0.96 1:2.5333
1.5 1.8 0.83 1:1.2000
2.125 1.8 1.12 1:0.8471
1.5 0.94 0.77 1:0.6267
2.125 0.94 1.06 1:0.4424
48hrs 2.625 - - -
- 15 - -
1.5 7.5 1.07 1:5.0000
1.5 3.8 0.82 1:2.5333
2.125 3.8 1.06 1:1.7882
2.125 1.8 0.93 1:0.8471
2.625 1.8 1.12 1:0.6857
2.125 0.94 0.87 1:0.4424
2.625 0.94 0.94 1:0.3581
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Table=2
Ca: ppm AI of MONTALINE C40 (cocamidopropyl-N-2-hydroxyethylcarbamoyl
methyl dimethyl ammonium chloride)
Cb: ppm AI of MBIT(N-methyl-1,2-benzisothiazolin-3-one)
Ratio:Ca:Cb
Test Organisms Contact Ca Cb S.I. Ca:Cb
Time
A. niger 3 days 650 - - -
ATCC # 16404 - 37.5 - -
20 18.8 0.53 1:0.9400
30 18.8 0.55 1:0.6267
42.5 18.8 0.57 1= 0. 442 4
87.5 18.8 0.64 1:0.2149
110 18.8 0.67 1:0.1709
200 18.8 0.81 1:0.0940
300 18.8 0.96 1:0.0627
425 18.8 1.16 1:0.0442
87.5 9.4 0.39 1:0.1074
110 9.4 0.42 1:0.0855
200 9.4 0.56 1:0.0470
300 9.4 0.71 1:0.0313
425 9.4 0.90 1:0.0221
525 9.4 1.06 1:0.0179
425 4.7 0.78 1:0.0111
525 4.7 0.93 1:0.0090
650 4.7 1.13 1:0.0072
425 2.4 0.72 1:0.0056
525 2.4 0.87 1:0.0046
650 2.4 1.06 1:0.0037
7 days 650 - -
- 75 -
0.2 37.5 0.50 1:187.5000
2 37.5 0.50 1:18.7500
20 37.5 0.53 1:1.8750
42.5 37.5 0.57 1:0.8824
65 37.5 0.60 1:0.5769
87.5 37.5 0.63 1:0.4286
110 37.5 0.67 1:0.3409
200 37.5 0.81 1:0.1875
300 37.5 0.96 1:0.1250
425 37.5 1.15 1:0.0882
110 18.8 0.42 1:0.1709
200 18.8 0.56 1:0.0940
300 18.8 0.71 1:0.0627
425 18.8 0.90 1:0.0442
525 18.8 1.06 1:0.0358
200 9.4 0.43 1:0.0470
300 9.4 0.59 1:0.0313
425 9.4 0.78 1:0.0221
525 9.4 0.93 1:0.0179
650 9.4 1.13 1:0.0145
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425 4.7 0.72 1:0.0111
525 4.7 0.87 1:0.0090
650 4.7 1.06 1:0.0072
C.albicans 48 hrs 525 - - -
ATCC # 10231 - 30 - -
300 15 1.07 1:0.0500
425 7.5 1.06 1:0.0176
425 3.75 0.93 1:0.0088
425 1.86 0.87 1:0.0044
425 0.94 0.84 1:0.0022
525 0.94 1.03 1:0.0018
72 hrs 1100 - - -
- 30 - -
87.5 30 0.67 1:0.3429
110 30 0.71 1:0.2727
200 30 0.88 1=0.1500
300 30 1.07 1:0.1000
300 15 0.82 1:0.0500
425 15 1.06 1:0.0353
425 7.5 0.93 1:0.0176
525 7.5 1.13 1:0.0143
425 3.75 0.87 1:0.0088
525 3.75 1.06 1:0.0071
425 1.86 0.84 1:0.0044
525 1.86 1.03 1:0.0035
525 0.94 1.02 1:0.0018
Ps. aeruginosa 24hrs 300 - - -
ATCC#9027 - 125 - -
87.5 75 0.89 1:0.8571
110 75 0.97 1:0.6818
200 37.5 0.97 1:0.1875
300 37.5 1.3 1:0.1250
200 18.75 0.82 1:0.0938
300 18.75 1.15 1:0.0625
200 9.4 0.74 1:0.0470
300 9.4 1.08 1:0.0313
300 4.6 1.04 1:0.0153
300 2.3 1.02 1:0.0077
48hrs 300 - -
- 125 - -
87.5 75 0.89 1:0.8571
110 75 0.97 1:0.6818
200 37.5 0.97 1:0.1875
300 37.5 1.3 1:0.1250
200 18.75 0.82 1:0.0938
300 18.75 1.15 1:0.0625
200 9.4 0.74 1:0.0470
300 9.4 1.08 1:0.0313
300 4.6 1.04 1:0.0153
300 2.3 1.02 1:0.0077
S.aureus 24hrs 5 - - -
ATCC#6538 15 - -
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14
2.188 7.5 0.94 1:3.4278
2.75 3.8 0.80 1:1.3818
3.8 1.25 1:0.7600
5 1.8 1.12 1:0.3600
5 0.94 1.06 1:0.1880
48hrs 5 - - -
- 15 -
2.188 7.5 0.94 1:3.4278
2.75 3.8 0.80 1:1.3818
5 3.8 1.25 1:0.7600
5 1.8 1.12 1:0.3600
5 0.94 1.06 1:0.1880
Table :3
Ca: ppm AI of ACQ type D (Cu(II) 2-aminoethanolate & didecyldimethyl
ammonium chloride) (ppm CuO)
5 Cb: ppm AI of MBIT(N-methyl-1,2-benzisothiazolin-3-one)
Ratio:Ca:Cb
Test Organisms Contact Ca Cb S.I. Ca:Cb
Time
A. niger 3 days 42.5 - - -
ATCC # 16404 - 37.5 -
2 18.8 0.55 1:9.4000
5.25 18.8 0.62 1:3.5810
6.5 18.8 0.65 1:2.8923
11 18.8 0.76 1:1.7091
20 18.8 0.97 1:0.9400
20 9.4 0.72 1:0.4700
30 9.4 0.96 1:0.3133
20 4.7 0.6 1:0.2350
30 4.7 0.83 1:0.1567
42.5 4.7 1.13 1:0.1106
20 2.4 0.53 1:0.1200
30 2.4 0.77 1:0.0800
42.5 2.4 1.06 1:0.0565
7 days 42.5 - - -
- 75 - -
2 37.5 0.55 1:18.7500
4.25 37.5 0.60 1:8.8235
6.5 37.5 0.65 1:5.7692
11 37.5 0.76 1:3.4091
20 37.5 0.97 1:1.8750
6.5 18.8 0.4 1:2.8923
11 18.8 0.51 1:1.7091
20 18.8 0.72 1:0.9400
30 18.8 0.96 1:0.6267
42.5 4.7 1.06 1:0.1106
42.5 1.2 1.02 1:0.0282
C.albicans 48 hrs 8.75 - - -
ATCC # 10231 - 30 - -
CA 02637129 2008-07-09
0.525 15 0.56 1:28.5714
1.1 15 0.63 1:13.6364
2 15 0.73 1:7.5000
4.25 15 0.99 1:3.5294
4.25 7.5 0.74 1:1.7647
6.5 7.5 0.99 1:1.1538
5.25 3.75 0.73 1:0.7143
6.5 3.75 0.87 1:0.5769
8.75 3.75 1.13 1:0.4286
5.25 1.86 0.66 1:0.3543
6.5 1.86 0.80 1:0.2862
8.75 1.86 1.06 1:0.2126
6.5 0.94 0.77 1:0.1446
8.75 0.94 1.03 1:0.1074
72 hrs 11 - - -
- 60
0.3 30 0.53 1:100.0000
1.1 30 0.6 1:27.2727
2 30 0.68 1:15.0000
4.25 30 0.89 1:7.0588
5.25 30 0.98 1:5.7143
6.5 30 1.09 1:4.6154
2 15 0.43 1:7.5000
2 15 0.43 1:7.5000
4.25 15 0.64 1:3.5294
5.25 15 0.73 1:2.8571
6.5 15 0.84 1:2.3077
8.75 15 1.05 1:1.7143
4.25 7.5 0.51 1:1.7647
5.25 7.5 0.6 1:1.4286
6.5 7.5 0.72 1:1.1538
8.75 7.5 0.92 1:0.8571
11 7.5 1.13 1:0.6818
5.25 3.75 0.54 1:0.7143
6.5 3.75 0.65 1:0.5769
8.75 3.75 0.86 1:0.4286
11 3.75 1..06 1:0.3409
6.5 1.86 0.62 1:0.2862
8.75 1.86 0.83 1:0.2126
11 1.86 1.03 1:0.1691
6.5 0.94 0.61 1:0.1446
8.75 0.94 0.81 1:0.1074
11 0.94 1.02 1:0.0855
Ps. aeruginosa 24hrs 20 - - -
ATCC#9027 - 75 - -
2 37.5 0.60 1:18.7500
3 37.5 0.65 1:12.5000
4.25 37.5 0.71 1:8.8235
5.25 37.5 0.76 1:7.1429
6.5 37.5 0.83 1:5.7692
8.75 37.5 0.94 1:4.2857
11 37.5 1.05 1:3.4091
CA 02637129 2008-07-09
16
5.25 18.75 0.51 1:3.5714
6.5 18.75 0.58 1:2.8846
8.75 18.75 0.69 1:2.1429
11 18.75 0.80 1:1.7045
20 18.75 1.25 1:0.9375
8.75 9.4 0.56 1:1.0743
11 9.4 0.68 1:0.8545
20 9.4 1.13 1:0.4700
11 4.6 0.61 1:0.4182
20 4.6 1.06 1:0.2300
20 2.3 1.03 1:0.1150
48 hrs 30 - - -
- 125 - -
0.425 75 0.61 1:176.4706
0.525 75 0.62 1:142.8571
1.1 75 0.64 1:68.1818
2 75 0.67 1:37.5000
4.25 75 0.74 1:17.6471
6.5 75 0.82 1:11.5385
11 75 0.97 1:6.8182
3 37.5 0.40 1:12.5000
4.25 37.5 0.44 1:8.8235
6.5 37.5 0.52 1:5.7692
11 37.5 0.67 1:3.4091
20 37.5 0.97 1:1.8750
8.75 18.75 0.44 1:2.1429
11 18.75 0.52 1:1.7045
20 18.75 0.82 1:0.9375
30 18.75 1.15 1:0.6250
20 9.4 0.74 1:0.4700
S.aureus 24hrs 1.1 - - -
ATCC#6538 - 15 - -
0.425 7.5 0.89 1:17.6471
0.525 7.5 0.98 1:14.2857
0.875 3.8 1.05 1:4.3429
0.875 1.8 0.92 1:2.0571
0.875 0.94 0.86 1:1.0743
1.1 0.94 1.06 1:0.8545
48hrs 1.1 - - -
- 15
0.525 7.5 0.98 1:14.2857
0.875 3.8 1.05 1:4.3429
1.1 0.94 1.06 1:0_ 8545
CA 02637129 2008-07-09
17
Table:4
Ca: ppm AI of CARBOQUAT WP-50(didecyl dimethyl ammonium carbonate and
bicarbonate)
Cb: ppm AI of MBIT(N-methyl-1,2-benzisothiazolin-3-one)
Ratio=Ca:Cb
Test Organisms Contact Ca Cb S.I. Ca:Cb
Time
A. niger 3 days 15 - - -
ATCC # 16404 - 37.5 - -
1 18.8 0.57 1:18.8000
2.125 18.8 0.64 1:8.8471
3.25 18.8 0.72 1:5.7846
4.375 18.8 0.79 1:4.2971
5.5 18.8 0.87 1:3.4182
18.8 1.17 1:1.8800
4.375 9.4 0.54 1:2.1486
5.5 9.4 0.62 1:1.7091
10 9.4 0.92 1:0.9400
7 days 32.5 - - -
- 37.5 -
1 18.8 0.53 1:18.8000
2.125 18.8 0.57 1:8.8471
3.25 18.8 0.60 1:5.7846
4.375 18.8 0.64 1:4.2971
5.5 18.8 0.67 1:3.4182
10 18.8 0.81 1:1.8800
18.8 0.96 1:1.2533
26.25 9.4 1.06 1:0.3581
21.25 4.7 0.78 1:0.2212
26.25 4.7 0.93 1:0.1790
32.5 4.7 1.13 1:0.1446
32.5 2.4 1.06 1:0.0738
C.albicans 48 hrs 3.25 - - -
ATCC # 10231 - 30 - -
2.125 15 1.15 1:7.0588
2.125 7.5 0.90 1:3.5294
3.25 7.5 1.25 1:2.3077
2.125 3.75 0.78 1:1.7647
3.25 3.75 1.13 1:1.1538
2.125 1.86 0.72 1:0.8753
3.25 1.86 1.06 1:0.5723
3.25 0.94 1.03 1:0.2892
72 hrs 4.375 - - -
- 60 - -
0.2625 30 0.56 1:114.2857
0.55 30 0.63 1:54.5455
1 30 0.73 1:30.0000
1.5 30 0.84 1:20.0000
2.125 30 0.99 1:14.1176
2.125 15 0.74 1:7.0588
CA 02637129 2008-07-09
18
3.25 15 0.99 1:4.6154
2.625 7.5 0.73 1:2.8571
3.25 7.5 0.87 1:2.3077
4.375 7.5 1.13 1:1.7143
2.625 3.75 0.66 1:1.4286
3.25 3.75 0.81 1:1.1538
4.375 3.75 1.06 1:0.8571
2.625 1.86 0.63 1:0.7086
3.25 1.86 0.77 1:0.5723
4.375 1.86 1.03 1:0.4251
3.25 0.94 0.76 1:0.2892
4.375 0.94 1.02 1:0.2149
Ps. aeruginosa 24hrs 10 - - -
ATCC#9027 - 125 - -
0.4375 75 0.64 1:171.4286
1 75 0.70 1:75.0000
1.5 75 0.75 1:50.0000
2.625 75 0.86 1:28.5714
3.25 75 0.93 1:23.0769
4.375 75 1.04 1:17.1429
4.6 1.04 1:0.4600
10 2.3 1.02 1:0.2300
48 hrs 10 - -
- 125 - -
2.125 75 0.81 1:35.2941
2.625 75 0.86 1:28.5714
3.25 75 0.93 1:23.0769
4.375 75 1.04 1:17.1429
10 4.6 1.04 1:0.4600
10 2.3 1.02 1:0.2300
S.aureus 24hrs 0.2125 - - -
ATCC#6538 - 15 - -
0.033 7.5 0.66 1:227.2727
0.055 7.5 0.76 1:136.3636
0.1 7.5 0.97 1:75.0000
0.15 3.8 0.96 1:25.3333
0.2125 0.94 1.06 1:4.4235
0.2125 - - -
- 15 - -
0.2125 0.94 1.06 1:4.4235
CA 02637129 2008-07-09
19
Table :5
Ca: ppm AI of ACQ C2 (Cu(II) 2=aminoethanolate) (ppm CuO)
Cb: ppm AI of MBIT(N-methyl-1,2-benzisothiazolin-3-one)
Ratio:Ca:Cb
Test Organisms Contact Ca Cb S.I. Ca:Cb
Time
A.nlger 3 days 425 - - -
ATCC # 16404 - 37.5 -
11 18.8 0.53 1:1.7091
20 18.8 0.55 1:0.9400
30 18.8 0.57 1:0.6267
42.5 18.8 0.60 1:0.4424
65 18.8 0.65 1:0.2892
87.5 18.8 0.71 1:0.2149
110 18.8 0.76 1:0.1709
200 18.8 0.97 1:0.0940
30 9.4 0.32 1:0.3133
42.5 9.4 0.35 1:0.2212
65 9.4 0.40 1:0.1446
87.5 9.4 0.46 1:0.1074
110 9.4 0.51 1:0.0855
200 9.4 0.72 1:0.0470
300 9.4 0.96 1:0.0313
87.5 4.7 0.33 1:0.0537
110 4.7 0.38 1:0.0427
200 4.7 0.60 1:0.0235
300 4.7 0.83 1:0.0157
425 4.7 1.13 1:0.0111
300 1.2 0.74 1:0.0040
425 1.2 1.03 1:0.0028
7 days 650 - -
- 37.5 - -
42.5 18.8 0.57 1:0.4424
65 18.8 0.60 1:0.2892
87.5 18.8 0.64 1:0.2149
110 18.8 0.67 1:0.1709
200 18.8 0.81 1:0.0940
300 18.8 0.96 1:0.0627
425 18.8 1.16 1:0.0442
42.5 9.4 0.32 1:0.2212
65 9.4 0.35 1:0.1446
87.5 9.4 0.39 1:0.1074
110 9.4 0.42 1:0.0855
200 9.4 0.56 1:0.0470
300 9.4 0.71 1:0.0313
425 9.4 0.90 1:0.0221
87.5 4.7 0.26 1:0.0537
110 4.7 0.29 1:0.0427
200 4.7 0.43 1:0.0235
300 4.7 0.59 1:0.0157
425 4.7 0.78 1:0.0111
CA 02637129 2008-07-09
525 4.7 0.93 1:0.0090
650 4.7 1.13 1:0.0072
200 2.4 0.37 1:0.0120
300 2.4 0.53 1:0.0080
425 2.4 0.72 1:0.0056
525 2.4 0.87 1:0.0046
650 2.4 1.06 1:0.0037
C.albicans 48 hrs 300
ATCC # 10231 - 60 - -
3 30 0.51 1:10.0000
11 30 0.54 1:2.7273
20 30 0.57 1:1.5000
42.5 30 0.64 1:0.7059
87.5 30 0.79 1:0.3429
110 30 0.87 1:0.2727
200 30 1.17 1:0.1500
0.525 15 0.25 1:28.5714
3 15 0.26 1:5.0000
11 15 0.29 1:1.3636
20 15 0.32 1:0.7500
42.5 15 0.39 1:0.3529
87.5 15 0.54 1:0.1714
110 15 0.62 1:0.1364
200 15 0.92 1:0.0750
6.5 7.5 0.15 1:1.1538
11 7.5 0.16 1:0.6818
20 7.5 0.19 1:0.3750
42.5 7.5 0.27 1:0.1765
87.5 7.5 0.42 1:0.0857
110 7.5 0.49 1:0.0682
200 7.5 0.79 1:0.0375
300 7.5 1.13 1:0.0250
11 3.75 0.10 1:0.3409
20 3.75 0.13 1:0.1875
42.5 3.75 0.20 1:0.0882
87.5 3.75 0.35 1:0.0429
110 3.75 0.43 1:0.0341
200 3.75 0.73 1:0.0188
300 3.75 1.06 1:0.0125
300 1.86 1.03 1:0.0062
300 0.94 1.02 1:0.0031
72 hrs 300 - - -
- 60 - -
3 30 0.51 1:10.0000
11 30 0.54 1:2.7273
20 30 0.57 1:1.5000
42.5 30 0.64 1:0.7059
87.5 30 0.79 1:0.3429
110 30 0.87 1:0.2727
200 30 1.17 1:0.1500
0.525 15 0.25 1:28.5714
3 15 0.26 1:5.0000
CA 02637129 2008-07-09
21
11 15 0.29 1:1.3636
20 15 0.32 1:0.7500
42.5 15 0.39 1:0.3529
87.5 15 0.54 1:0.1714
110 15 0.62 1:0.1364
200 15 0.92 1:0.0750
6.5 7.5 0.15 1:1.1538
11 7.5 0.16 1:0.6818
20 7.5 0.19 1:0.3750
42.5 7.5 0.27 1:0.1765
87.5 7.5 0.42 1:0.0857
110 7.5 0.49 1:0.0682
200 7.5 0.79 1:0.0375
300 7.5 1.13 1:0.0250
11 3.75 0.10 1:0.3409
20 3.75 0.13 1:0.1875
42.5 3.75 0.20 1:0.0882
87.5 3.75 0.35 1:0.0429
110 3.75 0.43 1:0.0341
200 3.75 0.73 1:0.0188
300 3.75 1.06 1:0.0125
300 1.86 1.03 1:0.0062
300 0.94 1.02 1:0.0031
Ps. aeruginosa 24hrs 110 - - -
ATCC#9027 - 75 - -
0.875 37.5 0.51 1:42.8571
2 37.5 0.52 1:18.7500
4.25 37.5 0.54 1:8.8235
8.75 37.5 0.58 1:4.2857
11 37.5 0.60 1:3.4091
20 37.5 0.68 1:1.8750
30 37.5 0.77 1:1.2500
42.5 37.5 0.89 1:0.8824
52.5 37.5 0.98 1:0.7143
65 37.5 1.09 1:0.5769
4.25 18.75 0.29 1:4.4118
8.75 18.75 0.33 1:2.1429
11 18.75 0.35 1:1.7045
20 18.75 0.43 1:0.9375
30 18.75 0.52 1:0.6250
42.5 18.75 0.64 1:0.4412
52.5 18.75 0.73 1:0.3571
65 18.75 0.84 1:0.2885
87.5 18.75 1.05 1:0.2143
30 9.4 0.40 1:0.3133
42.5 9.4 0.51 1:0.2212
52.5 9.4 0.60 1=0.1790
65 9.4 0.72 1:0.1446
87.5 9.4 0.92 1:0.1074
110 9.4 1.13 1:0.0855
42.5 4.6 0.45 1:0.1082
52.5 4.6 0.54 1:0.0876
CA 02637129 2008-07-09
22
65 4.6 0.65 1:0.0708
87.5 4.6 0.86 1:0.0526
110 4.6 1.06 1:0.0418
48 hrs 200 - - -
125 - -
0.2 75 0.60 1:375.0000
2 75 0.61 1:37.5000
4.25 75 0.62 1:17.6471
8.75 75 0.64 1:8.5714
11 75 0.66 1:6.8182
20 75 0.70 1:3.7500
30 75 0.75 1:2.5000
42.5 75 0.81 1:1.7647
52.5 75 0.86 1:1.4286
65 75 0.93 1:1.1538
87.5 75 1.04 1:0.8571
4.25 37.5 0.32 1:8.8235
8.75 37.5 0.34 1:4.2857
11 37.5 0.36 1:3.4091
20 37.5 0.40 1:1.8750
30 37.5 0.45 1:1.2500
42.5 37.5 0.51 1:0.8824
52.5 37.5 0.56 1:0.7143
65 37.5 0.63 1:0.5769
87.5 37.5 0.74 1:0.4286
110 37.5 0.85 1:0.3409
200 37.5 1.30 1:0.1875
42.5 18.75 0.36 1:0.4412
52.5 18.75 0.41 1:0.3571
65 18.75 0.48 1:0.2885
87.5 18.75 0.59 1:0.2143
110 18.75 0.70 1:0.1705
200 18.75 1.15 1:0.0938
42.5 9.4 0.29 1:0.2212
52.5 9.4 0.34 1:0.1790
65 9.4 0.40 1:0.1446
87.5 9.4 0.51 1:0.1074
110 9.4 0.63 1:0.0855
200 9.4 1.08 1:0.0470
87.5 4.6 0.47 1:0.0526
110 4.6 0.59 1:0.0418
200 4.6 1.04 1:0.0230
110 2.3 0.57 1:0.0209
200 2.3 1.02 1:0.0115
S.aureus 24hrs 52.5 - - -
ATCC#6538 - 15 - -
0.875 7.5 0.52 1:8.5714
1.1 7.5 0.52 1:6.8182
2 7.5 0.54 1:3.7500
4.25 7.5 0.58 1:1.7647
6.5 7.5 0.62 1:1.1538
11 7.5 0.71 1:0.6818
CA 02637129 2008-07-09
23 20 7.5 0.88 1:0.3750
30 7.5 1.07 1:0.2500
11 3.8 0.46 1:0.3455
20 3.8 0.63 110.1900
30 3.8 0.82 1:0.1267
42.5 3.8 1.06 1:0.0894
30 1.8 0.69 1:0.0600
42.5 1.8 0.93 1:0.0424
52.5 1.8 1.12 1:0.0343
42.5 0.94 0.87 1:0.0221
52.5 0.94 1.06 1:0.0179
48hrs 65 - - -
- 15 - -
2 7.5 0.53 1:3.7500
4.25 7.5 0.57 1:1.7647
6.5 7.5 0.6 1~ 1.1538
8.75 7.5 0.63 1:0.8571
11 7.5 0.67 1:0.6818
20 7.5 0.81 1:0.3750
30 7.5 0.96 1:0.2500
42.5 7.5 1.15 1:0.1765
20 3.8 0.56 1:0.1900
30 3.8 0.71 1:0.1267
42.5 3.8 0.91 1:0.0894
52.5 3.8 1.06 1:0.0724
65 1.8 1.12 1:0.02 7 7
65 0.94 1.06 1:0.0145
Table:6
Ca: ppm AI of CAPMUL GML(glycerol monolaurate)
Cb: ppm AI of MBIT(N-methyl-1,2-benzisothiazolin-3-one)
Ratio:Ca:Cb
Test Organisms Contact Ca Cb S.I. Ca:Cb
Time
A. niger 3 days 11000 - - -
ATCC # 16404 - 37.5 - -
200 18.8 0.52 1:0.0940
425 18.8 0.54 1:0.0442
650 18.8 0.56 1:0.0289
1100 18.8 0.60 1:0.0171
2000 18.8 0.68 1:0.0094
3000 18.8 0.77 1:0.0063
4250 18.8 0.89 1:0.0044
5250 18.8 0.98 1:0.0036
6500 18.8 1.09 1:0.0029
1100 9.4 0.35 1:0.0085
2000 9.4 0.43 1:0.0047
3000 9.4 0.52 1:0.0031
4250 9.4 0.64 1:0.0022
5250 9.4 0.73 1:0.0018
CA 02637129 2008-07-09
24
6500 9.4 0.84 1:0.0014
11000 4.7 1.13 1:0.0004
11000 2.4 1.06 1:0.0002
7 days 11000 -
- 37.5 - -
2000 18.8 0.68 1:0.0094
3000 18.8 0.77 1:0.0063
4250 18.8 0.89 1:0.0044
5250 18.8 0.98 1:0.0036
6500 18.8 1.09 1:0.0029
1100 18.8 0.60 1:0.0171
11000 9.4 1.25 1:0.0009
11000 4.7 1.13 1:0.0004
11000 2.4 1.06 1:0.0002
C. albicans 48 hrs 11000 - -
ATCC # 10231 - 30 - -
525 15 0.55 1:0.0286
875 15 0.58 1:0.0171
1100 15 0.60 1:0.0136
2000 15 0.68 1:0.0075
3000 15 0.77 1:0.0050
4250 15 0.89 1:0.0035
5250 15 0.98 1:0.0029
6500 15 1.09 1:0.0023
4250 7.5 0.64 1:0.0018
5250 7.5 0.73 1:0.0014
6500 7.5 0.84 1:0.0012
8750 7.5 1.05 1:0.0009
5250 3.75 0.60 1:0.0007
6500 3.75 0.72 1:0.0006
8750 3.75 0.92 1:0.0004
11000 3.75 1.13 1:0.0003
5250 1.86 0.54 1:0.0004
6500 1.86 0.65 1:0.0003
8750 1.86 0.86 1:0.0002
11000 1.86 1.06 1= 0. 0002
11000 0.94 1.03 1:0.0001
72 hrs 11000 - - -
- 30 - -
1100 15 0.60 1:0.0136
2000 15 0.68 1:0.0075
3000 15 0.77 1:0.0050
4250 15 0.89 1:0.0035
5250 15 0.98 1:0.0029
6500 15 1.09 1:0.0023
5250 7.5 0.73 1:0.0014
6500 7.5 0.84 1:0.0012
8750 7.5 1.05 1:0.0009
11000 1.86 1.06 1:0.0002
11000 0.94 1.03 1:0.0001
Ps. aeruginosa 24hrs 11000 - - -
ATCC#9027 - 125 - -
CA 02637129 2008-07-09
525 75 0.65 1:0.1429
650 75 0.66 1:0.1154
875 75 0.68 1:0.0857
1100 75 0.70 1:0.0682
2000 75 0.78 1:0.0375
3000 75 0.87 1:0.0250
4250 75 0.99 1:0.0176
S:aureus 24hrs 650 - -
ATCC#6538 - 15 - -
300 7.5 0.96 1:0.0250
400 7.5 1.12 1:0.0188
48hrs 2000 - - -
15 - -
300 7.5 0.65 1:0.0250
650 7.5 0.83 1:0.0115
875 7.5 0.94 1:0.0086
1100 7.5 1.05 1:0.0068
Table :7
Ca: ppm AI of CAPMUL PG12 (propylene glycol mono-laurate)
Cb: ppm AI of MBIT(N-methyl-1,2-benzisothiazolin-3-one)
5 Ratio:Ca=Cb
Test Organisms Contact Ca Cb S.I. Ca:Cb
Time
A. niger 3 days 1100 - - -
ATCC # 16404 - 37.5 - -
110 18.8 0.60 1:0.1709
200 18.8 0.68 1:0.0940
300 18.8 0.77 1:0.0627
425 18.8 0.89 1:0.0442
525 18.8 0.98 1:0.0358
650 18.8 1.09 1:0.0289
1100 2.4 1.06 1:0.0022
7 days 1100 - - -
- 75 - -
300 37.5 0.77 1:0.1250
425 37.5 0.89 1:0.0882
525 37.5 0.98 1:0.0714
1100 2.4 1.03 1:0.0022
C.albicans 48 hrs 1100 - -
ATCC # 10231 30 -
52.5 15 0.55 1:0.2857
110 15 0.60 1:0.1364
200 15 0.68 1:0.0750
300 15 0.77 1:0.0500
425 15 0.89 1:0.0353
525 15 0.98 1:0.0286
650 15 1.09 1:0.0231
1100 0.94 1.03 1:0.0009
72 hrs 1100 - - -
CA 02637129 2008-07-09
26
- 30 - -
52.5 15 0.55 1:0.2857
110 15 0.60 1:0.1364
200 15 0.68 1:0.0750
300 15 0.77 1:0.0500
425 15 0.89 1:0.0353
525 15 0.98 1:0.0286
650 15 1.09 1:0.0231
1100 0.94 1.03 1:0.0009
Table=8
Ca: ppm Al of CAPMUL PG8 (propylene glycol caprylate)
Cb: ppm AI of MBIT(N-methyl-1,2-benzisothiazolin-3-one)
Ratio:Ca:Cb
Test Organisms Contact Ca Cb S.I. Ca:Cb
Time
A. niger 3 days 875 - - -
ATCC # 16404 - 37.5 - -
42.5 18.8 0.55 1:0.4424
65 18.8 0.58 1:0.2892
87.5 18.8 0.60 1:0.2149
110 18.8 0.63 1:0.1709
200 18.8 0.73 1:0.0940
300 18.8 0.84 1:0.0627
425 18.8 0.99 1:0.0442
425 9.4 0.74 1:0.0221
525 9.4 0.85 1:0.0179
650 9.4 0.99 1:0.0145
525 4.7 0.73 1:0.0090
650 4.7 0.87 1:0.0072
875 4.7 1.13 1:0.0054
650 2.4 0.81 1:0.0037
875 2.4 1.06 1:0.0027
650 1.2 0.77 1:0.0018
875 1.2 1.03 1:0.0014
7 days 1100 -
- 75 - -
525 37.5 0.98 1:0.0714
650 37.5 1.09 1:0.0577
650 18.8 0.84 1:0.0289
875 18.8 1.05 1:0.0215
875 9.4 0.92 1:0.0107
1100 9.4 1.13 1:0.0085
875 4.7 0.86 1:0.0054
1100 4.7 1.06 1:0.0043
875 2.4 0.83 1:0.0027
1100 2.4 1.03 1:0.0022
1100 1.2 1.02 1:0.0011
CA 02637129 2008-07-09
27 C: albicans 48 hrs 200 - - -
ATCC # 10231 - 30 - -
65 15 0.83 1:0.2308
87.5 15 0.94 1:0.1714
110 15 1.05 1:0.1364
110 7.5 0.80 1:0.0682
200 3.75 1.13 1:0.0188
200 1.86 1.06 1:0.0093
200 0.94 1.03 1:0.0047
72 hrs 200 - - -
- 30 - -
65 15 0.83 1:0.2308
87.5 15 0.94 1:0.1714
110 15 1.05 1:0.1364
200 0.94 1.03 1:0.0047
